Data / Medical devices / Lamp, Infrared, Therapeutic Heating / Italy
FDA-registered makers of Lamp, Infrared, Therapeutic Heating in Italy: 5 establishments
5 establishments in Italy are registered with the FDA to make Lamp, Infrared, Therapeutic Heating (product code ILY). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Lamp, Infrared, Therapeutic Heating
- Product code
- ILY
- Country
- Italy
Makers of Lamp, Infrared, Therapeutic Heating in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Fisioline S.R.L. | VERDUNO Cuneo, Italy | Manufacturer | 4 | July 26, 2016 | 0 | 0 | 0 | api.fda.gov |
| Asa S.R.L. | ARCUGNANO Vicenza, Italy | Manufacturer | 2 | November 9, 2011 | 0 | 0 | 0 | api.fda.gov |
| Eltech K-Laser S.R.L. | Treviso, Italy | Contract manufacturer, Manufacturer | 1 | May 25, 2012 | 0 | 0 | 0 | api.fda.gov |
| El.en. Electronic Engineering SPA | CALENZANO Firenze, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mectronic Medicale S.R.L. | Grassobbio Bergamo, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.